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Objectives: The chemical composition and toxicity of wintertime urban-air particulate matter with an aerodynamic diameter of <10 microm (PM10), derived mostly from long-range transport and local combustion sources, were compared with those of springtime PM10 derived mostly from the resuspension of road dust., Methods: Water-soluble ions and elements and polycyclic aromatic hydrocarbons (PAH) were analyzed from seasonally pooled PM10 samples collected at a busy traffic site in Helsinki in 1999. These PM10 samples were also tested for cytotoxicity [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide test] and the production of proinflammatory cytokines [tumor necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6)] and nitric oxide (NO) in the mouse macrophage cell line RAW 264.7. Their oxidative capacity and the associated DNA (deoxyribonucleic acid) damage were investigated by electron paramagnetic resonance and the formation of 8-hydroxy-2'-deoxyguanosine (8-OH-DG) in isolated calf thymus DNA, respectively., Results: The late wintertime and springtime PM10 had similar compositions of water-soluble ions and elements, but the winter PM10 had a higher content of PAH. The spring PM10 was a much more potent inducer of TNF-alpha and IL-6 production than the winter PM10 was, but there were no consistent differences in cytotoxic potency. In contrast, the winter PM10 was a significantly more potent inducer of NO production and 8-OH-DG formation. The large cytokine responses to the spring PM10 were caused by its insoluble fraction and largely inhibited by the endotoxin antagonist polymyxin B. The transition metal chelator deferoxamine did not modify the proinflammatory or cytotoxic responses to the PM10 samples., Conclusions: The toxicity profile of urban-air PM10 changed with season in a subarctic climate. Particulate-bound endotoxin from soil gram-negative bacteria is suggested as a highly proinflammatory constituent of springtime resuspended road dust.

An ion chromatographic method for the detemination of inorganic anions in Herba Ephedrae was developed. The separation of the anions was achieved on a Shim-Pack IC-AI column with a mixture of 2.5 mmol/L phthalic acid and 2.4 mmol/L tris (hydroxymethyl) amino-methane as mobile phase, and the detection was performed by a conductivity detector. Fluoride, chloride, nitrite, bromide, nitrate and sulfate could be identified within 10 min. The method is simple and useful, and has good linearity with correlation coefficients between 0.999 2 and 0.999 7 and relative standard deviations lower than 1.92%. The recoveries of anions in the samples were between 96.6% and 100.4%.

Study on limnobiotic status of the Fort lake water was made to assess the potability of water from Feb 1998 to Jan 1999. Fort lake exhibits high alkalinity with pH ranging from 8.36 (June) to 10.6 (Feb and March), total alkalinity (TA) from 88 to 188 mg/l, total hardness (TH) from 59.8-217 mg/l, PO4 (7.2 to 13.6 mg/l and BOD (42.6-60.6 mg/l). From the observations it can be known that the Fort lake water is inferior and not suitable for drinking purposes. The possible factors for its poor quality have been discussed.

The elemental composition and particle size distribution of suspended particles in raw water, treated water, and distributed water were determined to understand the behavior of particles during the water treatment-distribution process. The weight of suspended particles collected on a 0.6-microm filter was 1.1 times (raw water), 1.4 times (treated water), and 1.5 times (distributed water) that collected on a 2.7-microm filter, suggesting that smaller particles may remain after conventional water treatment. Organic suspended particles were removed less efficiently than inorganic suspended particles. After sand filtration, the Al content in the fixed suspended solids (FSS) markedly increased, indicating that either a small percentage of aluminium floc passed through during sand filtration or dissolved aluminum precipitated after sand filtration. The Mn and Fe concentrations increased after chlorination. The percentages of carbon and nitrogen in the volatile suspended solids (VSS) were roughly the same in the raw, treated, and distributed waters. The carbon/nitrogen/phosphate/VSS ratios indicated that the VSS of the suspended particles consisted of organic matter originating from microorganisms. The major constituents of the FSS in the treated and distributed waters were compounds of Fe, Al, Ca, Mg, and Mn, but these compounds accounted for only 16% or less of the FSS in raw water, indicating the existence of Si compounds. In distribution pipes, the total suspended solids concentration, especially the FSS concentration, was higher than that of water just after treatment. The Fe concentration in distributed water increased, probably due to oxidation and rusting of iron pipes.

Sewage sludge is a serious problem due to the high treatment costs and the risks to environment and human health. Future sludge treatment will be progressively focused on an improved efficiency and environmental sustainability of the process. In this context a survey is given of the most relevant sludge treatment options and separate treatment steps. Special attention is paid to those processes that are simultaneously focused on the elimination of the risks for environment and human health and on the recovery or beneficial use of the valuable compounds in the sludge such as organic carbon compounds, inorganic non-toxic substances, phosphorus and nitrogen containing compounds. Also, a brief assessment is given of the specific future technological developments regarding the various treatment steps. Furthermore, it is discussed how to assess the various pathways which can lead to the required developments. In such an assessment the technical and economic feasibility, the environmental sustainability, the societal acceptance and the implementation route are important factors. The optimal approach also strongly depends on the local and regional situation of concern and the relevant current and future boundary conditions.

The present study aims to analyze the interaction of prevailing biotic pressure on soil environment with emphasis on its physicochemical and microbiological characteristics determining soil fertility status and thus supporting plant and animal biodiversity in Nanda Devi Biosphere Reserve (NDBR) which is located in northern part of Uttaranchal hills between 79 degrees 40'E to 80 degrees 05'E longitude and 30 degrees 17'N to 30 degrees 41'E latitude. The experimental results revealed that the physico-chemical characteristics (viz., moisture, pH, EC, C, N, P, K, CEC) of soil were maximum in moderately grazed meadow and minimum in intensively grazed meadow. Soil microbial analysis measured in terms of total viable count (TVC) exhibited grazing sensitivity trend being maximum population of bacteria > fungi > actinomycetes. The soil microbial population was positively correlated with soil respiration, dehydrogenase activity, acid phosphatase and microbial biomass, which exhibited uneven trend with grazing pressure. Soil from moderately grazed meadow showed highest microbial count and enzyme activities, whilst intensively grazed meadow showed lowest microbial count and enzyme activities. This depicts the beneficial role of prescribed grazing up to limited extent in management of soil fertility, which might have supported luxuriant growth of a variety of grasses.

Water-soluble macromolecular polyacids can play a potentially important role in the hygroscopic properties of atmospheric aerosols. These acids have molecular structures similar to natural fulvic acids (FA) (or humic acids) and are referred to as humic-like substances (HULIS). In this study, the hygroscopicity of HULIS and the mixture of HULIS and sodium chloride (NaCl) and that of HULIS and ammonium sulfate (AS) aerosols at a mass ratio of 1:1 are studied using two natural FA: the Nordic Aquatic Fulvic Acid (NAFA) and the Suwannee River Fulvic Acid (SRFA) as model compounds in an electrodynamic balance. NAFA and SRFA both absorbed and desorbed water reversibly without crystallization and retained water at a relative humidity (RH) < 10%. NAFA and SRFA have a mass growth ratio of 1.25 and 1.45 from RH = 10% to RH = 90%, respectively. However, these results are different from those of another natural FA (the Nordic River Fulvic Acid Reference) in the literature. The differences are possibly due to the differences in the chemical composition of the natural FA, which depends on their sources and the isolation methods. These results suggest that a standardization of the isolation methods of HULIS is needed for better understanding of their atmospheric properties and environmental impacts. In general, the deliquescence and crystallization RH of FA-inorganic mixtures are comparable with those of their respective pure inorganic species. Since FA are less hygroscopic than NaCl and AS, all mixtures absorb less water compared to their respective pure inorganic species of equal particle mass. The FA-AS mixtures have a larger water uptake than the sum of those of the FA and AS individually following a simple additivity rule as noninteracting species at RH = 90%. This enhancement effect increases as the RH decreases. There is no such enhancement effect for the FA-NaCl mixtures until RH is below 90%. These results reveal that the effect of the interactions between FA and inorganic species on the water uptake of the mixtures, in general, is a function of RH.

The potential of near-infrared (NIR) spectroscopy to measure the main inorganic components of seawater as salt-manufacturing materials was investigated. A total of 72 seawater samples collected from six locations was used, and spectra (1100-1800 nm) were acquired by a NIR spectrophotometer with a 1-mm path length. Principal component analysis (PCA), canonical correlation analysis (CCA), and partial least-squares (PLS) regression were performed based on the reference inorganic components. As a result, the principal component analysis and canonical correlation analysis showed that the near-infrared spectra could be related to the inorganic components of seawater. The partial least-squares regression analysis showed that the inorganic components (ion concentration of Cl, Na+, K+, SO4(2-), and Ca2+) could be predicted with good accuracy using NIR spectra and their second derivatives. For Cl ion and K+ ion concentrations, the accuracy was high.

Atmospheric aerosols were sampled at a coastal site and analyzed for H+, NH+4, Ca++, Mg++, Na+, SO4- -, HCO(-3), Cl- and No3-. The analysis demonstrated that these ions are the main constituents of the aerosols sampled. The correlation coefficients are calculated for each possible pair of anions and cations. Ionic balance in the ambient aerosols indicate that the main compounds existed are in the order of sodium chloride; bicarbonates of calcium and magnesium; sulphates of sodium, magnesium and calcium; and nitrates of sodium, magnesium and calcium. The existence of cations has exceeded the anions which indicate that ionic composition of the aerosols are not very much determined by background marine nature but may also be due to transport of polluted air masses from the surrounding areas.

A review is presented detailing the development and use of suppression devices for the conductimetric detection of inorganic ions by ion chromatography (IC). An overview of the general response equation for conductivity detection is also given. Topics of discussion include the role and function of suppressors, the development of early suppressors including packed column and membrane devices from 1975 to 1990 and the subsequent progression towards present day commercially available suppressors and recent innovations. Post-suppression devices for signal enhancement are also discussed.

Capillary electrophoresis microchip devices are receiving considerable attention due to their versatility, portability, and sample handling capabilities. This article is a comprehensive review of the analysis of inorganic and small, charged organic species on microchip platforms. The application of conductivity, amperometry, laser-induced fluorescence, absorbance, and chemiluminescence detection methods are discussed. The potential utilization of these devices for miniaturized analytical systems is described.

The purpose of this work was to study the distribution of airborne particles in the surroundings of an iron and steel factory in southern Finland. Several sources of particulate emissions are lying side by side, causing heavy dust loading to the environment. This complicated multi-pollutant situation was studied mainly by SEM/EDX methodology. Particles accumulated on Scots pine bark were identified and quantitatively measured according to their element content, size and shape. As a result, distribution maps of particulate elements were drawn and the amount of different particle types along the study lines was plotted. Particulate emissions from the industrial or energy production processes were not the main dust source. Most emissions were produced from the clinker crusher. Numerous stockpiles of the industrial wastes and raw materials also gave rise to particulate emissions as a result of wind erosion. It was concluded that SEM/EDX methodology is a useful tool for studying the distribution of particulate pollutants.

In this work, using a combination of experimental design (ED) and artificial neural networks (ANN), the composition of a triethanolamine-buffered chromate electrolyte was optimised for determination of sulphate anions in the presence of high chloride excess. The optimal electrolyte, allowing a baseline-resolved separation of sulphate from chloride present in a 1500 multiple excess in less than 170 s, consists of 10 mmol/L CrO(3), 2 mmol/L hexamethonium hydroxide, 10% methanol, and triethanolamine added to adjust the pH to 8.0. The method is suitable to a wide concentration range of chloride (4-1757 mg/L) and sulphate (4-590 mg/L) with linear calibration plots (R(2) = 0.9937-0.9999). Relative standard deviations are less than 2.0% for both anions for migration times and peak areas. The detection limits (hydrodynamic injection of 1 s) were 0.6 mg/L for sulphate and 0.5 mg/L for chloride. The method was successfully applied to determination of sulphate in mineral waters containing a high chloride concentration and to determination of sulphate traces in an anticancer drug injection preparation containing a physiological level of chloride. It was shown that alpha-cyclodextrin as an electrolyte additive has a significant potential for further increasing the separation selectivity for inorganic anions.

Concentrations of inhalable particulate matter (PM10), Pb, Zn, Pt, Ce, Cd, Se and of Benzo(a)pyrene (BaP) were determined in three locations near Venice from September 2000 to September 2001. Meteorological conditions were considered during the sampling period. All components showed higher concentrations during winter, except for Cd and Se in the two sites at Mestre. Spatial and temporal variations were observed. There were correlations between Pb and Zn and PM10, Cd and Se, Pb and BaP and, in the main street sampling site, also between BaP and Pt. Their possible sources of emission are discussed on the basis of correlations among elements.

Analytical results are reported for the determination of inorganic species in water and sediments sampled in the Lamone and Marzeno rivers ecosystem. The species determined are Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Zn, Hg, F-, Cl- Br-, NO3-, SO4--, Na+, K+, Mg++, Ca++, NH4+ in superficial water, and Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Zn, Hg in sediments. For all the elements, in addition to detection limits, precision and accuracy are given: the former, expressed as relative standard deviation (s(r)), and the latter, expressed as relative error (e), were good, being in all cases lower than 6%.

Analysis of organic and inorganic compounds in plasma, epidermal tissue and cuticle were accomplished in the intermolt (C3 stage) of crab Scylla serrata incubated in different pH media. Significant changes with similar trends for protein, carbohydrates, glycosaminoglycans (GAG), sulphur, calcium, magnesium, potassium, phosphorus and copper in the plasma suggested higher dissolution in an acidic medium while the deposition increased in alkaline medium. Similar decreases in protein, carbohydrate and GAG in the epidermal compartment were observed from pH 4 to pH 12. However, significantly higher contents of sodium, chloride, potassium, phosphorus, magnesium, sulphur and copper were measured at pH 7.5 with a symmetrical decrease profile in both acidic and alkaline media, resulting from synergistic effects in the osmotic regulation. Clear changes in calcium concentrations were observed with a sharp increase from lower contents at pH 7.5 to higher at pH 12. In the cuticle, the acidic condition induced a significant dissolution of HCl-protein, GAG, calcium and magnesium contents. On the other hand, the alkaline condition induced a significant decrease in carbohydrate, calcium, chloride, sulphur and potassium. A reduction trend is seen for NaOH and H(2)O-protein contents in the cuticle. These observations suggest that GAG and HCl-protein might constitute the most soluble fraction with high affinity for calcium binding and easily removed in acidic conditions. Additionally, it is possible to speculate that the carbohydrates associated with the NaOH and H(2)O-proteins may form an interface between the soluble matrix fraction and the chitin framework. Sulphur groups seem to present a strong linkage role in this interface fraction, maybe only broken by a specific enzyme in extreme alkaline conditions with subsequent release of significant calcium from the shell., (Copyright 2003 Wiley-Liss, Inc.)

Microbial life in the harsh conditions of Antarctica's cold desert may be considered an analogue of potential life on early Mars. In order to explore the development and survival of this epilithic and endolithic form of microbial life, our most sophisticated, state-of-the-art visualization technologies have to be used to their full potential. The study of any ecosystem requires a knowledge of its components and the processes that take place within it. If we are to understand the structure and function of each component of the microecosystems that inhabit lithic substrates, we need to be able to quantify and identify the microorganisms present in each lithobiontic ecological niche and to accurately characterize the mineralogical features of these hidden microhabitats. Once we have established the techniques that will allow us to observe and identify these microorganisms and mineral substrates in situ, and have confirmed the presence of water, the following questions can be addressed: How are the microorganisms organized in the fissures or cavities? Which microorganisms are present and how many are there? Additional questions that logically follow include: What are the existing water relationships in the microhabitat and what effects do the microorganisms have on the mineral composition? Mechanical and chemical changes in minerals and mineralization of microbial cells can give rise to physical and/or chemical traces (biomarkers) and to microbial fossil formation. In this report, we describe the detection of chains of magnetite within the Martian meteorite ALH84001, as an example of the potential use of SEM-BSE in the search for plausible traces of life on early Mars.

Capillary electrophoresis (CE) continues its invasion into the domain of inorganic analysis. This review summarizes the progress and significant developments of CE of inorganic ions over the first two years of the new century. As manifested by the substantial number of published articles, this field is still witnessing a growing activity of many separation scientists. To provide an in-depth treatment of fundamental and methodological aspects of inorganic ion analysis by CE, an extensive fraction of the relevant literature is covered whereas only most innovative application reports are briefly considered. Most of the recent advancements have focused on CE system modernization designed to improve a limited detection sensitivity, which still remains a major obstacle to overcome in order to ensure the method's wider practical acceptance. Attention is also given to how and in which directions the future research could be performed to implement CE in routine inorganic analysis.

The purpose of this study was to evaluate the correlation between degree of conversion and microhardness in dental composites, as well as the effect of the inorganic content and type of photo-curing unit on these parameters. Three indirect composites (Artglass, Solidex and Zeta LC) were polymerized by means of three different laboratorial units (UniXS, Solidilite and an experimental device). For each material, fifteen samples were prepared using a metal matrix. The degree of conversion was analyzed by means of infrared spectroscopy, and microhardness was also assessed. The inorganic content was measured by means of thermogravimetric analysis (TGA). The Pearson s test was carried out in order to determine correlations. The degree of conversion of Artglass ranged from 37.5% to 79.2%, and its microhardness, from 32.4 to 50.3 (r = 0.904). The degree of conversion of Solidex ranged from 41.2% to 60.4%, and its microhardness, from 33.3 to 44.1 (r = 0.707). The degree of conversion and the microhardness of Zeta LC ranged from 62.0% to 78.0% and from 22.6 to 33.6, respectively (r = 0.710). It was concluded that the utilization of different photo-curing units caused variations on the degree of conversion, as a result of specific characteristics of each unit. For each material, there was strong correlation between the degree of conversion and microhardness. In addition, when different materials were compared, microhardness was more affected by filler content than by the degree of conversion.

Analytical results are reported for the determination of inorganic species in water and sediments sampled in the Aso river ecosystem. The species determined are Cd, Co, Cr, Cu, Fe, Mn, Ni, Zn, Hg, F-, NO3-, SO4--, Na, K, Ca, Mg, NH4+ in water, and Cd, Co, Cr, Cu, Fe, Mn, Ni, Zn, Hg in sediments. For all the elements, in addition to detection limits, precision and accuracy are given: the former, expressed as relative standard deviation (Sr), and the latter, expressed as relative error (e), were good, being in all cases lower than 6%.

The losses of nutrients by fire were assessed in a Trachypogon savanna located in Calabozo, Venezuela. About 95% of the biomass, 97% of N, 61% of P, 76% of K and 65% of Ca and Mg were transferred to the atmosphere. Ash deposition returned between 21-34% of Mg, Ca, K and P and 0.2% of N. Previous data indicated that precipitation and atmospheric fixation (in the case of N) could replace the rest of N, Ca, K and Mg transferred to the atmosphere. As a consequence of frequent burning (annual or biannual), the soil of the savanna showed lower organic matter and available P and K content when it is compared with a 32 year protected savanna.

Background: Occupational exposures may be related to the development of brain cancer. The objective was to estimate occupational-specific risk of gliomas and meningiomas among Swedish men and women gainfully employed in 1970 over the period 1971-1989, and the influence of occupational exposure to chemical substances., Methods: A dataset linking cancer diagnoses from the Swedish national cancer register to occupational and demographical data obtained in the 1970 census was used to fit log-linear Poisson models, in order to obtain relative risks adjusted by age, period, geographical area and town size. Exposure to 13 chemicals was assessed using a Swedish job-exposure matrix., Results: The main findings of this study among men were the increased risk of glioma with occupational exposure to arsenic, mercury, and petroleum products and of meningioma with lead. Women in occupational sectors with a higher socio-economic status showed an increased incidence of both, gliomas and meningiomas., Conclusions: Occupational exposure to some chemicals appeared to be related with an increased risk of glioma and meningioma in men. Exposures involved in glioma and meningioma development seemed to be different., (Copyright 2002 Wiley-Liss, Inc.)

This paper describes the combined use of a new preconcentration method using the Amberlite IRA-743 resin and high-performance liquid chromatography coupled to inductively coupled plasma mass spectrometry to determine simultaneously inorganic and organic selenium species in aquatic systems. The developed enrichment procedure, whose accuracy has been checked by recovery tests, is suitable for selenium speciation at environmental levels of 10 ng (Se) l(-1). The method has been applied to mineral and freshwater samples.

A new application of capillary electrophoresis (CE) for measuring inorganic anions in hailstones was carried out. Five hailstone specimens were collected from large blocks of ice that fell in January 2000 in some provinces of Spain. Sample handling and preparation procedures were performed with care. CE analysis of anions was carried out using indirect UV detection at 254 nm with a negative power supply (-15 kV) and hydrostatic injection (10 cm for 30 s) at 35 degrees C. Anion separation was completed in less than 4 min. The working electrolyte consisted of 4.7 mM sodium chromate, 4.0 mM OFM-OH (tetradecyltrimethylammonium hydroxide), 10 mM CHES [2-(N-cyclohexylamino)ethanesulfonic acid], and 0.1 mM calcium gluconate (pH 9.1). Good repeatability of migration times after eight injections (<0.7% RSD), adequate linearity responses (r2>0.9) as well as satisfactory detection limits (<0.35 ppm) were achieved. The analytical results provided by CE were compared with those obtained by traditional wet-chemical (WCH) methods. Most of the results obtained by CE were consistent with those of WCH, except for one sample.

Capillary electrophoretic separations of inorganic anions are performed using a capillary coated with a mixture of the cationic surfactant didodecyldimethylammonium bromide (DDAB) and the zwitterionic surfactant 1,2-dilauroyl-sn-phosphatidylcholine (DLPC). These double-chained surfactants form semi-permanent coatings on the capillary wall, which allows the excess surfactant to be removed from the buffer prior to separation. Interactions between surfactant aggregates in the buffer and analyte anions are thus eliminated. The electroosmotic flow (EOF) can be altered from fully reversed (100% DDAB) to near zero (100% DLPC) using different ratios of DDAB and DLPC. Controlling the EOF allows for improved resolution of the anions while maintaining a rapid, co-EOF separation, free from analyte-surfactant additive interactions.

An identification procedure connected with selection of candidates for identification according to high values of their literature citation and cocitation is suggested. The citation rate of the compound is the number of different literature units, such as papers, patents, etc., recording its name. The cocitation rate is the number of such units mutually recording the names of two corresponding compounds or the compound and the sample/matrix. General citation of a chemical compound is assumed to be related to the prior probability of its being contained in a sample to be analyzed. This citation measures abundance and popularity of the compound. Cocitation of a compound with a known/identified constituent of a sample is related to their mutual similarity in structure or properties, origin, use, etc. This data processing method is validated by counting citations and cocitations for detected impurities in pure n-hexane and naphthalene, polycyclic aromatic hydrocarbons in waste gas, as compared with counts for similar or dissimilar compounds that are absent in the samples. The analytes are preidentified by combined gas chromatography and mass spectrometry techniques. A median and a mean value of citation and cocitation are always higher for the group of unambiguously identified compounds. A difference between identified and similar compounds in citations or cocitations may be rather insignificant, with combined evaluation of both indicators distinguishing these groups. Chemical dissimilarity results in a large difference in cocitation values.

The Residue on Ignition Test specified in General Tests, Japanese Pharmacopeia is a method to measure the weight of the residual substance not volatilized when the sample is ignited under a constant condition. Generally, this test is intended to determine the content of inorganic substances contained as impurities in an organic substance, and, occasionally, to determine the amount of inorganic substances contained as components in an organic substance. Our laboratories have adopted this test method for the above two purposes in the case of the quality control for drug substances, synthetic intermediates, starting materials in the course of drug development. Some validation studies have been conducted for this test in order to clarify the quantitation limit in the case of an application for the former purpose, and trueness and precision in the case of the latter purpose. Consequently, the quantitation limit was determined as around 0.50 mg. The amount of sample should be determined based on this quantitation limit (mg) and the level of quantitation limit (%) or that of specification limit (%) should be considered from the view point of each testing purpose. The test method was also confirmed to have a good trueness and precision as the determination method for an alkaline salt, such as sodium, potassium or calcium salt, of organic compounds, as long as the test is operated with great care not to scatter the content out of crucible during ignition to incineration.

In respect of their rapidity, their online capabilities, and their moderate costs, biosensing systems generally offer an attractive alternative to the existing methods of water analysis. Additionally, one particular advantage of microbial biosensors is the ability to measure direct effects on living cells, e.g., their respiratory activity and its alteration caused by environmental pollutants. It is true that microbial sensors, often do not provide the optimum solution for the determination of individual analytes when compared to established physico-chemical analysis methods. However, these biosensing devices are predestined for the summary determination of environmentally relevant compounds and their complex effects, respectively. For this reason, microbial sensors allow an integral evaluation of the degree of environmental pollution including the interaction of various compounds. Moreover, in some cases specific metabolic pathways in microorganisms are used, resulting in the development of microbial sensors for the more selective analysis for those compounds or pollutants, which cannot be measured by simple enzyme reactions, e.g., the determination of aromatic compounds and heavy metals. This chapter gives an overview of microbiological biosensors on respiratory basis for the measurement of the following environmentally relevant compounds: inorganic N-compounds, heavy metals, organic xenobiotics and the estimation of sum parameters or so-called complex parameters such as BOD, ADOC, N-BOD, and the inhibition of nitrification.

The review deals with the problems of development of analytical equipment based on piezoelectric crystals. Consideration is given to the philosophy of determining inorganic and organic compounds, biologically active compounds, viruses, and bacteria with piezoelectric resonators. Described are methods of immobilization of the biological component, immersion-and-drying analysis, and sensor-assisted detection in the soluble phase.

Micro-electrodes were applied to anaerobic granular sludge, which was developed in a UASB reactor, to examine intra-granule profiles with respect to pH, glucose and sulfide. When glucose was employed as a bulk liquid substrate, the micro-electrodes study demonstrated the pH behavior along granule depth: pH decrement at the granule exterior portion due to acid formation (buildup of acidity), and subsequent pH increment at the granule inner portion due to the consumption of acid (buildup of alkalinity). Sulfide micro-electrode proved sulfate reduction that mostly occurred at the granule exterior portion. Chemical equilibrium consideration evidently explained the occurrence of ferric sulfide predominantly in the interior portion, which accounts well for the morphology of a representative double-layered structure of granules grown on a low level of sulfite. Inorganic elements distribution within anaerobic granule was examined by electron probe X-ray micro analysis (EPMA) and ICP methods. The presence of crystalline calcium carbonate (calcite) was identified by X-ray diffraction analysis.

One of the major problems facing the development of capillary electrophoresis (CE) is the relatively high limits of detection when compared to traditional high-performance liquid chromatographic (HPLC) methods. While the use of an alternative detector can offer better sensitivity, a more universal approach is sample preconcentration. Numerous on-line methods have been developed to improve the sensitivity of CE, and are based on electrophoretic principles, chromatographic principles, or a combination of both. This review will discuss all forms of on-line preconcentration methods for CE, with emphasis given to those that have shown particular merit when applied to inorganic and small organic anions.

Organic and inorganic anions in snow and ice from Glacier 1 at Urumqi river head, Tianshan Mountain, Xinjiang, Northwest China, were determined using DIONEX-300 ion chromatograph with a lot of columns. AS4A-SC was selected as the separation column, AG4A-SC as the guard column, TAC-2 as the anion enrichment column, ATC-1 as the anion trap column and ASRS-II as the suppresser. It was conducted under gradient elution with sodium tetraborate (Na2B4O7) as eluent and 25 mmol/L H2SO4 as regeneration solution for chemical suppression. By preconcentration, 2 mL melted water of snow or ice can be analyzed for separation and quantitation of more than 10 anions, which were fluoride, acetate, formate, pyruvate, monochloroacetate, chloride, nitrite, bromide, nitrate, phosphate, sulfate and oxalate. The relative standard deviations for most of the anions were below 5%.

The present investigation provides data of some ions, namely Na+, Ca2+, NH4+, Cl-, NO3-, CN- and PO4(3-) on water samples of river Osun, selected rivers in the region and groundwaters. The pH, temperature, electrical conductivity (EC), total dissolved solids (TDS), total hardness (TH) and total carbon (IV) oxide (TCO2) have also been determined to asses the chemical status and pollution levels of these water sources. The higher values of certain parameters with respect to the acceptable standard limits for drinking water indicate the pollution in both groundwater and river water samples of the study area, and make the waters unsuitable for various applications. The high pollution river water source showed higher levels of phosphate, nitrate and ammonium ions (P < 0.05). There is no significant difference (P < 0.05) between the mean concentrations of other inorganic nutrients in the high and low pollution water source types. The correlation coefficient between quality parameter pairs of river water and groundwater samples are determined and the significance of these parameters in both types of water sources are discussed.

A non-suppressed ion chromatographic method with conductometric detection is described for the simultaneous determination of six inorganic anions: fluoride, chloride, nitrite, bromide, nitrate and sulphate. The separation was achieved on a low-capacity anion-exchange column Metrohm IC Anion Column Super Sep, with a mobile phase consisting of phtalic acid dissolved in high-purity water, 2-amino-2-hydroxymethyl-1,3-propendiol and acetonitrile. In this work computer optimization procedures, using computer programs to select chromatographic conditions have been used, leading to the achievement of a desired separation. By using the different optimization methods in an integrated manner it is, however, possible to both speed method development, by reducing unnecessary experimentation, and to overcome the many shortcomings of each method, because of the different approaches. The purpose of this work is to improve and characterise the method for simultaneous determination of six inorganic anions in drinking water by non-suppressed ion chromatography, using optimization procedures, in order to be applied to the routine analysis. The proposed method has numerous advantages over the other widely used non-suppressed ion chromatography methods: higher selectivity, shorter analysis time, lower quantitation and detection limits. The performance characteristics of the method were established by determining the following validation parameters: precision and accuracy, linearity, detection limits and quantitation limits.

The technique of microdialysis enables the monitoring of neurotransmitters and other molecules in the extracellular environment. This method has undergone several modifications and is now widely used for sampling and quantitating neurotransmitters, neuropeptides, and hormones in the brain and periphery. This unit describes the principles of conventional and quantitative microdialysis as well as strategies in designing a dialysis experiment. It establishes the groundwork for the basic techniques of preparation, conduct, and analysis of dialysis experiments in rodents and subhuman primates. Although the methods described are those used for monitoring CNS function, they can be easily applied with minor modification to other organ systems.

By using a fine oil-filled glass microcapillary mounted on a micromanipulator, the solutes of individual plant cells can be sampled. These samples can then be analysed using a range of physical and chemical methods. Hydrostatic pressure (cell pressure probe), osmotic pressure (picolitre osmometer), organic solutes (enzyme-linked fluorescence microscope spectrometry or capillary electrophoresis), inorganic solutes (X-ray microdroplet analysis or capillary electrophoresis), (14)C (mass spectrometry), proteins (microdroplet immunoblotting), and mRNA (rt PCR) have been measured. Collectively, the battery of techniques is called single cell sampling and analysis (SiCSA) and all of the techniques have relevance to the study of plant metabolism at the resolution of the individual cell. This review summarizes the techniques for SiCSA and presents examples of applications used in this laboratory, in particular those relating to cell metabolism.

The 10 kinds of inorganic elements were determined in 12 kinds of Chinese traditional medicines. The relation showed that there were numerous inorganic elements in the traditional chinese medicines. The relation between these inorganic elements and the efficacies of these medicines was studied and the efficacies of these Chinese traditional medicines were discussed. The efficacies of these traditional medicines were greatly influenced by the content of inorganic elements. To guarantee the efficacies of these traditional medicines, the reasonable control lines concerned with the content of inorganic elements shall be established and the lines will be discussed in the future.

This study uses scanning ultraviolet-visible (UV-Vis) spectrophotometer to monitor natural organic matter (NOM) in water. The results showed that the area under the UV-Vis spectra is a good surrogate to monitor the concentration of the aqueous NOM. No apparent difference was found between the spectra of the three commercially available humic acids used in this study. The use of the scanning spectra compensates the potential random error in the absorbance determined at single wavelength due to the heterogeneous NOM compositions. The major interference of the proposed method comes from the formazine turbidity and nitrate nitrogen (NO3- -N). Although filtration with a 0.45-microm filter can remove most of the interference from formazine, some interference is still present at a wavelength less than 250 nm. Also it is found that the presence of the NO3- -N greatly affect the spectra of the NOM. In order to monitor the NOM in water with minimized interference, it is recommended that the area under the spectra between 250 and 350 nm should be used as a surrogate for concentration of NOM in water.

The application of indirect spectrophotometric detection was investigated for a capillary electrochromatographic system in which an anion-exchange stationary phase (in the form of aminated latex particles) was coated onto the wall of a fused-silica capillary. The study has focused on the choice of the type and concentration of the absorbing coion (probe) added to the background electrolyte and the role of this species in manipulating the ion-exchange contributions to the separation with a view to controlling the selectivity of the separation. Common inorganic anions were used as analytes and nitrate, p-toluenesulfonate, nicotinate, and chromate were investigated as probes. It was found that most of these probes produced only a limited range of separation selectivities when their concentration was varied over the practically accessible range. p-Toluenesulfonate provided the greatest variation in selectivity, but peak distortion due to electromigration dispersion was evident for the faster ions. When variation of the separation selectivity - from predominantly electrophoretic in nature to predominantly ion-exchange in nature - was desired, this was best achieved by varying the type of probe rather than its concentration. For example, the nitrate probe provided predominantly electrophoretic separations with good peak shapes and high efficiencies. A comprehensive list of probes, ranked in order of ion-exchange selectivity coefficients determined by ion chromatography, was compiled and this proved to be a useful tool to assist in the selection of a probe for a desired separation selectivity. The limits of detection for the analytes and probes studied ranged from 20-55 micromol for the chromate system to 230-600 micromol for the nicotinate system, with nitrate and p-toluenesulfonate giving intermediate values.

The method for analysis of inorganic cations in brine solutions was developed. Ion chromatography is a well-established and accepted technique in the determination of a variety of inorganic ions. However, there are significant complications when ion chromatography is used to determine trace concentrations of inorganic ions in brine matrices. The brine solution in our study was made to simulate the solution from the Waste Isolation Pilot Plant. Instrumental parameters such as eluent composition, flow-rates, and sample loop volumes were investigated to arrive at the optimum condition for the determination of the cations with minimal dilution. Separation was carried out in a Dionex CG12A/CS12A with 8.25 mM H2SO4 as eluent at 1.2 ml/min flow-rate. Our results indicated that ion chromatography is an accurate and a good alternative method for the analysis of cations in brine solution.

US Environmental Protection Agency Method 300.0 specifies the use of an IonPac AS4A anion-exchange column with a carbonate-hydrogencarbonate eluent and suppressed conductivity detection for the determination of inorganic anions in environmental waters by ion chromatography. Hydroxide eluents have not typically been used for the routine analysis of common inorganic anions due to the lack of an appropriate hydroxide selective column and the difficulty in preparing contaminant free hydroxide eluents. The use of ion chromatography with a hydroxide-selective IonPac AS17 column, automated eluent generation and potassium hydroxide gradient represents a new approach to the routine determination of inorganic anions in environmental waters. This new approach, which is a modification of Method 300.0, allows equivalent method performance with improved linearity, precision, and method detection limits. The AS17 column provides superior retention of fluoride from the column void volume and improved resolution from small organic acids, such as formate and acetate, compared to the AS4A column. Quantitative recoveries were obtained for all the common inorganic anions spiked into typical environmental waters using this new approach, and the Performance Based Measurement System Tier 1 method validation quality control acceptance criteria are well within the acceptable ranges defined by Method 300.0. In addition, the EG40 eluent generator eliminates the need to manually prepare eluents, increasing the level of automation and ease-of-use of the ion chromatography system.

Which method should I use for ion analysis, ion chromatography (IC) or capillary electrophoresis (CE)? In terms of actual theoretical plates CE has a clear-cut advantage. The separation ability of IC is adequate for many sample types, and many separation scientists feel that IC offers greater reliability and confidence than CE. However, IC is a more mature technique and there has been more time to solve problems such as peak tailing and to improve reproducibility. The two techniques should be viewed as complementary. A number of recent developments in ion analysis by CE are discussed. These include some simple ways to control electroosmotic flow and improve reproducibility, separation of isotopes, improved methods of indirect photometric detection, a new contactless conductivity detector, separation of ions at low pH, and in solutions of high salt content. Progress in a new technique called IC-CE will be described in which a soluble ion-exchange polymer is added to the capillary electrolyte to separate anions based on differences in both electrophoretic mobility and ion-exchange interactions.

A minimal neural network was applied to a large library of high-temperature mobility spectra drawn from 16 chemical classes including 154 substances with 2000 spectra at various concentrations. A genetic algorithm was used to create a representative subset of points from the mobility spectrum as input to a cascade-type back-propagation network. This network demonstrated that significant information specific to chemical class was located in the spectral region near the reactant ions. This network failed to generalize the solution to unfamiliar compounds necessitating the use of complete spectra in network processing. An extended back-propagation network classified unfamiliar chemicals by functional group with a mean for average values of 0.83 without sulfides and 0.79 with sulfides. Further experiments confirmed that chemical class information was resident in the spectral region near the reactant ions. Deconvolution of spectra demonstrated the presence of ions, merged with the reactant ion peaks that originated from introduced samples. The ability of the neural network to generalize the solution to unfamiliar compounds suggests that these ions are distinct and class specific.

In the practice of forensic medicine, we find many of cases of death where the actual cause is not determinable with autopsy, histological or toxicological examinations. In these cases of death, we can consider cardiac dysfunction of unknown origin, in the background of which such a physiologic cardiac insufficiency occurs that cannot be detected with the previously mentioned methods. The dysfunction is possibly associated with a significant change in certain inorganic elements, primarily in the conduction system of the heart. In the absence of published data, our goal was to determine the concentration of inorganic elements in the specialized rhythm determining muscle cell groups in the heart: sinus node (SN), atrioventricular node (AV), septum (SE), left ventricle anterior wall (LVAW). With microwave technology we destroyed the muscle tissue and measured the concentration of ions (Na, Mg, K, Ca, Mn, Fe, Cu, Zn, P, S) using Inductive Completed Plasma Atom Emission Spectrometry (ICP-AES) equipment. Of the 24 cases examined, the average ion concentrations in microgram/g were the following; Sinus: Na 2602 +/- 493, Mg 120 +/- 24, K 1787 +/- 347, Ca 244 +/- 41, Mn 0.129 +/- 0.011, Fe 58 +/- 12, Cu 2.171 +/- 0.46, Zn 10.4 +/- 2.027, P 1147 +/- 227, S 2301 +/- 245; Septum: Na 1452 +/- 315, Mg 243 +/- 56, K 3269 +/- 689, Ca 105 +/- 26, Mn 0.17 +/- 0.05, Fe 74 +/- 16, Cu 3.557 +/- 0.952, Zn 25.75 +/- 8.4, P 2764 +/- 494, S 3001 +/- 523; Av: Na 2614 +/- 517, Mg 242 +/- 40.2, K 2010 +/- 395, Ca 271 +/- 27.3, Mn 0.13 +/- 0.029, Fe 54 +/- 12, Cu 2.369 +/- 0.297, Zn 15 +/- 3.2, P 1625 +/- 291, S 2535 +/- 346; Lvaw: Na 1340 +/- 201, Mg 250 +/- 37, K 3659 +/- 532, Ca 88 +/- 22, Mn 0.175 +/- 0.05, Fe 76 +/- 19, Cu 3.62 +/- 0.58, Zn 27.13 +/- 3.1, P 3025 +/- 441, S 3140 +/- 440.

This paper describes a simple processing and analysis scheme for explosives trace swab samples which deals both with organic and inorganic materials. Swabs, wetted with ethanol or ethanol/water mixture, were extracted with ethanol/water mixture. The extract was passed directly through a simple column containing an acrylonitrile/styrene copolymer adsorbent. The adsorbent retained common organic explosives, which were recovered with an efficiency of 30-50% as a relatively clean ethyl acetate solution. The concentrated ethyl acetate eluate was analysed using gas chromatography with chemiluminescence or mass spectrometric detection. The unretained inorganic ions and sugars, which were recovered with generally high efficiency as an ethanol/water solution, could be directly analysed using ion chromatography and/or capillary electrophoresis. Minor difficulties encountered in the analysis of sugars, fluoride and phosphate were examined.

Larval flannelmouth sucker (Catostomus latipinnis) were exposed to arsenate, boron, copper, molybdenum, selenate, selenite, uranium, vanadium, and zinc singly, and to five mixtures of five to nine inorganics. The exposures were conducted in reconstituted water representative of the San Juan River near Shiprock, New Mexico. The mixtures simulated environmental ratios reported for sites along the San Juan River (San Juan River backwater, Fruitland marsh, Hogback East Drain, Mancos River, and McElmo Creek). The rank order of the individual inorganics, from most to least toxic, was: copper > zinc > vanadium > selenite > selenate > arsenate > uranium > boron > molybdenum. All five mixtures exhibited additive toxicity to flannelmouth sucker. In a limited number of tests, 44-day-old and 13-day-old larvae exhibited no difference in sensitivity to three mixtures. Copper was the major toxic component in four mixtures (San Juan backwater, Hogback East Drain, Mancos River, and McElmo Creek), whereas zinc was the major toxic component in the Fruitland marsh mixture, which did not contain copper. The Hogback East Drain was the most toxic mixture tested. Comparison of 96-h LC50 values with reported environmental water concentrations from the San Juan River revealed low hazard ratios for arsenic, boron, molybdenum, selenate, selenite, uranium, and vanadium, moderate hazard ratios for zinc and the Fruitland marsh mixture, and high hazard ratios for copper at three sites and four environmental mixtures representing a San Juan backwater, Hogback East Drain, Mancos River, and McElmo Creek. The high hazard ratios suggest that inorganic contaminants could adversely affect larval flannelmouth sucker in the San Juan River at four sites receiving elevated inorganics.

General aspects of the deterioration and typical examples in some hot springs (Atami, Shirahama, Isawa.Kasugai, and Syuzenji Hot Springs) are outlined in this report in connection with the change of chemical constituents. (1) Deterioration of thermal spring resources generally occurs accompanied with the following phenomena: a) drawdown of the water level in thermal water wells. b) lowering of temperature of thermal springs. c) change of the water quality (salt water encroachment in the coastal region and decrease in concentration of chemical components resulting from the intrusion of underground water in the inland area). (2) Typical examples of the deterioration are summarized as follows; [table: see text] (3) It has been revealed from the analyses of the statistical data of Environment Agency that the deterioration of hot spring resources in Japan is gradually progressing.

The levels of salivary proteins and some inorganic elements were measured in healthy children who were divided into 3 groups according to dentition. The study was prompted by the fact that there have been few studies on salivary composition and most of them have measured only a few components in children. Salivary protein was determined by the method of Lowry; protein electrophoresis carried out as described by Laemli; Na and K concentration was measured by flame photometry and Ca, Mg, Cl and P measured colorimetrically using Randox diagnostic kits. Significant differences were found between the groups for Mg, Na, total protein and some protein bands (obtained by electrophoresis). In all dentition groups, there was no significant difference in any of the levels between the children with and without caries. Salivary inorganic composition, total protein concentration and some protein bands rose linearly with age. Salivary protein and all the above inorganic element levels rose linearly with total caries surface area (Ds + ds), except for Mg which decreased linearly. Some of the protein bands decreased with Ds + ds.